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Autosomaal recessieve aplasia cutis
Autosomaal recessieve cutis laxa type 2B
Chalastodermia
Chalazoderma
Chalazodermia
Chaloderma
Chalodermie
Corpus papillare
Corpus papillare cutis
Cutis laxa
Cutis laxa senilis
Cutis pendula
Cutis rhomboidalis nuchae
Dermatolyse
Dermatolysis
Pachydermatokèle
Sarcomatose
Sarcomatose cutis
Sarcomatosis cutis
Stratum papillare cutis
Xerosis cutis

Vertaling van "sarcomatose cutis " (Nederlands → Engels) :

sarcomatose cutis | sarcomatosis cutis

sarcomatosis cutis




corpus papillare | corpus papillare cutis | stratum papillare cutis

corpus papillare | corpus papillare corii


chalastodermia | chalazoderma | chalazodermia | chaloderma | chalodermie | cutis laxa | cutis pendula | dermatolyse | dermatolysis | pachydermatokèle

chalazodermia | cutis laxa | dermatolysis | loose skin | pachydermatocele


autosomaal recessieve aplasia cutis

An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to


autosomaal recessieve cutis laxa type 2B

Autosomal recessive cutis laxa type 2B










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Date index: 2022-09-20
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